Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

258806

Sigma-Aldrich

Mesoporphyrin IX dihydrochloride

synthetic, 95%

Synonym(s):

7,12-Diethyl-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-dipropionic acid dihydrochloride

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C34H38N4O4 · 2HCl
CAS Number:
68938-72-7
Molecular Weight:
639.61
EC Number:
273-141-0
MDL number:
MFCD00136049
UNSPSC Code:
12161600
PubChem Substance ID:
24855661
NACRES:
NA.22

Quality Level

100

Assay

95%

reaction suitability

core: porphyrin
reagent type: catalyst

λmax

401 nm

SMILES string

Cl.Cl.CCc1c(C)c2cc3[nH]c(cc4nc(cc5[nH]c(cc1n2)c(C)c5CCC(O)=O)c(CCC(O)=O)c4C)c(C)c3CC

InChI

1S/C34H38N4O4.2ClH/c1-7-21-17(3)25-13-26-19(5)23(9-11-33(39)40)31(37-26)16-32-24(10-12-34(41)42)20(6)28(38-32)15-30-22(8-2)18(4)27(36-30)14-29(21)35-25;;/h13-16,35,38H,7-12H2,1-6H3,(H,39,40)(H,41,42);2*1H/b25-13-,26-13-,27-14-,28-15-,29-14-,30-15-,31-16-,32-16-;;

InChI key

LLAQRSFKJHORNW-HXFTUNQESA-N

Application

Reactant in constructing efficient dye-sensitized solar cells

Product can be used with our line of photoreactors: Including Penn PhD (Z744035) & SynLED 2.0 (Z744080)

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCF9445
MKCC8195
MKBV0344V
MKBN3572V
MKBC8130V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Naoki Hosomi et al.
Journal of bioscience and bioengineering, 99(3), 222-229 (2005-10-20)
Monoclonal antibody 2D7 generated against a transition-state analog N-methyl mesoporphyrin catalyzes a reaction for insertion of a cupric ion into mesoporphyrin. To investigate amino acid residues responsible for the catalytic activity, site-directed mutagenesis of the amino acid residues in the
Shane C McAllister et al.
Pharmacogenomics, 6(3), 235-244 (2005-07-15)
Kaposi's sarcoma (KS) is a multifocal angioproliferative disorder affecting the skin, mucosa and viscera of individuals infected with human herpesvirus-8 (HHV-8; also Kaposi's sarcoma-associated herpesvirus [KSHV]). KS is the most common neoplasm in AIDS patients; the clinical outcome of AIDS-KS
Roxanne Kieltyka et al.
Methods in molecular biology (Clifton, N.J.), 608, 223-255 (2009-12-17)
Telomerase inhibition through guanine quadruplex sequestration by small-molecule drugs is of great current interest as an anticancer strategy. G-quadruplexes (GQs) can be formed at the guanine-rich sequences found at the end of the telomere. They possess a large electron-rich pi-surface
S Scheingraber et al.
European surgical research. Europaische chirurgische Forschung. Recherches chirurgicales europeennes, 42(3), 157-167 (2009-01-30)
The role of hemoxygenase (HO)-1 after partial liver resection (PLR) in jaundiced animals has yet to be defined. We therefore investigated: (1) the acute effects of bile duct ligation (BDL) on bilirubin accumulation and hepatocellular integrity after PLR; (2) how
Jesús Tejero et al.
The Biochemical journal, 433(1), 163-174 (2010-10-19)
NOSs (NO synthases, EC 1.14.13.39) are haem-thiolate enzymes that catalyse a two-step oxidation of L-arginine to generate NO. The structural and electronic features that regulate their NO synthesis activity are incompletely understood. To investigate how haem electronics govern the catalytic
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service